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pubmed-article:10743946pubmed:abstractTextRecent evidence is consistent with neurotensin (NT)(8-13) adopting a Type I beta-turn conformation while binding the NT receptor, which would place the cationic side-chains of Arg(8) and Arg(9) in close proximity. This was the basis for the design, synthesis and analysis of truncated NT(9-13) analogues 1-5 with dicationic position 9 side-chains to emulate the functions of the 8 and 9 side-chains of NT(8-13).lld:pubmed
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pubmed-article:10743946pubmed:articleTitleSynthesis of neurotensin(9-13) analogues exhibiting enhanced human neurotensin receptor binding affinities.lld:pubmed
pubmed-article:10743946pubmed:affiliationDepartment of Pharmaceutical Sciences, Medical University of South Carolina, Charleston 29425-2303, USA.lld:pubmed
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